CNVIntegrate: the first multi-ethnic database for identifying copy number variations associated with cancer

Human copy number variations (CNVs) and copy number alterations (CNAs) are DNA segments (>1000 base pairs) of duplications or deletions with respect to the reference genome, potentially causing genomic imbalance leading to diseases such as cancer. CNVs further cause genetic diversity in healthy p...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Database (Oxford)
Main Authors: Chattopadhyay, Amrita, Teoh, Zi Han, Wu, Chi-Yun, Juang, Jyh-Ming Jimmy, Lai, Liang-Chuan, Tsai, Mong-Hsun, Wu, Chia-Hsin, Lu, Tzu-Pin, Chuang, Eric Y
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2021
Teme:
Original Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8278790/
https://ncbi.nlm.nih.gov/pubmed/34259866
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/database/baab044
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